Effects of cyclohexenonic long-chain fatty alcohol in type 2 diabetic rat nephropathy

被引:4
|
作者
Okada, Shinichi [2 ]
Saito, Motoaki [1 ]
Kinoshita, Yukako
Satoh, Itaru
Kawaba, Yasuo [2 ]
Hayashi, Atsushi [2 ]
Oite, Takashi [3 ]
Satoh, Keisuke
Kanzaki, Susumu [2 ]
机构
[1] Tottori Univ, Dept Pathophysiol & Therapeut Sci, Div Mol Pharmacol, Fac Med, Yonago, Tottori 6838503, Japan
[2] Tottori Univ, Div Pediat & Perinatol, Fac Med, Yonago, Tottori 6838504, Japan
[3] Niigata Univ, Dept Cellular Physiol, Inst Nephrol, Grad Sch Med & Dent Sci,Chuo Ku, Niigata 9518150, Japan
来源
BIOMEDICAL RESEARCH-TOKYO | 2010年 / 31卷 / 04期
关键词
MESANGIAL CELL-PROLIFERATION; N-HEXACOSANOL; NEURONS; INJURY; MICE; MODEL; HYPERTENSION; DEFICIENCY; EXPRESSION; PODOCYTES;
D O I
10.2220/biomedres.31.219
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We attempted to clarify the effects of cyclohexenonic long-chain fatty alcohol (CHLFA) on the alterations of type 2 diabetes-induced nephropathy. Forty-week-old male Goto-Kakizaki (GK) and Wistar rats were divided into four groups of 6 to 8 animals. Group A consisted of eight Wistar rats and served as an age-matched control group. Group B (7 GK rats) received no treatment and served as a diabetic group. Group C (6 GK rats) was treated daily with low-dose CHLFA (2 mg/kg/body weight, subcutaneously) for 30 weeks, and Group D (6 GK rats) with high-dose CHLFA (8 mg/kg/body weight) for 30 weeks. At the end of the treatment period, urinary protein excretion, blood chemistry, renal histological, and immunohistological analyses were conducted. Although CHLFA administration did not influence serum glucose or insulin levels, it reversed diabetes-induced increases in urinary protein excretion and serum creatinine. Light microscopically, CHLFA treatment ameliorated the otherwise elevated glomerular sclerotic scores in the diabetic group. lmmunohistochemically, increased expression of desmin and decreased expression of rat endothelial cell antigen-1 in the group with untreated diabetes both showed a reversal to control levels in the high-dose CHLFA treatment group. In conclusion, CHLFA may ameliorate type 2 diabetes-induced nephropathy.
引用
收藏
页码:219 / 230
页数:12
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